Evidence map›Paper›PMID 31727941›Full record

ArticleScientific reports2019

Insufficient production of IL-10 from M2 macrophages impairs in vitro endothelial progenitor cell differentiation in patients with Moyamoya disease.

Eiichiro Nagata, Haruchika Masuda, Taira Nakayama, Shizuka Netsu, Hiroko Yuzawa, Natsuko Fujii, Saori Kohara, Takatoshi Sorimachi, Takahiro Osada, Ryoko Imazeki and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Eiichiro NagataDepartment of Neurology, Tokai University School of Medicine, Isehara, Japan. enagata@is.icc.u-tokai.ac.jp.ORCID http://orcid.org/0000-0001-6902-8309
Haruchika MasudaDepartment of Physiology, Tokai University School of Medicine, Isehara, Japan.ORCID http://orcid.org/0000-0001-7200-4586
Taira NakayamaDepartment of Neurology, Tokai University School of Medicine, Isehara, Japan.
Shizuka NetsuDepartment of Neurology, Tokai University School of Medicine, Isehara, Japan.
Hiroko YuzawaDepartment of Neurology, Tokai University School of Medicine, Isehara, Japan.
Natsuko FujiiDepartment of Neurology, Tokai University School of Medicine, Isehara, Japan.
Saori KoharaDepartment of Neurology, Tokai University School of Medicine, Isehara, Japan.
Takatoshi SorimachiDepartment of Neurosurgery, Tokai University School of Medicine, Isehara, Japan.
Takahiro OsadaDepartment of Neurosurgery, Tokai University School of Medicine, Isehara, Japan.
Ryoko ImazekiDepartment of Neurology, Tokai University School of Medicine, Isehara, Japan.
Mitsunori MatsumaeDepartment of Neurosurgery, Tokai University School of Medicine, Isehara, Japan.
Takayuki AsaharaDepartment of Basic Clinical Science, Division of Regenerative Medicine, Tokai University School of Medicine, Isehara, Japan.
Shunya TakizawaDepartment of Neurology, Tokai University School of Medicine, Isehara, Japan.
Tokai University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Moyamoya disease (MMD) is well known to be caused by insufficient cerebral vascular formation. However, the essential pathogenesis has not yet been identified. Using our recently developed technique of generating vasculogenic and anti-inflammatory cultures, we investigated endothelial progenitor cell (EPC) expansion and differentiation under the cytokine milieu generated by the peripheral blood mononuclear cells (PBMNCs) of the operated and non-operated MMD patients. EPC colony forming assay of the cultured PBMNCs disclosed the decline of the definitive EPC colony numbers in the both MMD patients. The level of interleukin-10 (IL-10) was lower in secretory cytokines from the cultured PBMNCs of MMD patients than that in that of controls using a cytometric bead array. The addition of human recombinant IL-10 to PBMNCs cultured from MMD patients restored the EPC colony forming potential of MMD PBMNCs. Following phorbol myristate acetate stimulation of the cultured PBMNCs, flow cytometry revealed a decrease in intracellular IL-10 storage in the main cell populations of the PBMNCs cultured from MMD patients relative to those cultured from controls. The present data provide the expected mechanism of vascular malformation in MMD pathogenesis originated from the insufficient production of IL-10 secreting cells from PBMNCs fostering EPC expansion and differentiation.

Indexed as

AdultCase-Control StudiesCell Culture TechniquesCell DifferentiationCells, CulturedColony-Forming Units AssayDown-RegulationEndothelial Progenitor CellsFemaleFlow CytometryHumansInterleukin-10Leukocytes, MononuclearMacrophagesMaleMiddle AgedIL10 protein, humanInterleukin-10Tetradecanoylphorbol Acetate

Identifiers

PMID31727941
PMCPMC6856135
OpenAlexW2984580500

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.